111011-76-8

Basic information

• Product Name: EFONIDIPINE
• Synonyms: Efonidipine hydrochloride monoethanolate;Efonidipine Hydrochloride ethanol (1:1:1);2-(phenyl(phenylmethyl)amino)ethyleste;3-pyridinecarboxylicacid,1,4-dihydro-2,6-dimethyl-5-(5,5-dimethyl-1,3,2-dioxa;efonidipinehydrochlorideethanolate;nz-105;nz105ethanolate;r,p-oxide,monohydrochloride
• CAS NO: 111011-76-8
• Molecular Formula: C34H38N3O7P
• Molecular Weight: 631.66
• Mol File: 111011-76-8.mol
• Article Data: 0

Chemical Properties

• Melting Point: 151° (dec)
• Boiling Point: 746.9 °C at 760 mmHg
• Flash Point: 405.5 °C
• Appearance: /
• Density: 1.3 g/cm³
• Vapor Pressure: 3.5E-22mmHg at 25°C
• Storage Temp.: Desiccate at +4°C
• CAS DataBase Reference: EFONIDIPINE(CAS DataBase Reference)
• NIST Chemistry Reference: EFONIDIPINE(111011-76-8)
• EPA Substance Registry System: EFONIDIPINE(111011-76-8)

Safety Data

• Hazardous Substances Data: 111011-76-8(Hazardous Substances Data)

Usage

Description

Efonidipine hydrochloride ethanol was first launched in Japan for the treatment of essential severe and renal hypertension. As the fourteenth dihydropyridine (DHP) calcium channel blocker to reach the market, it functions by binding to the DHP receptors on voltage-dependent calcium channels to cause diuretic and natriuretic actions in patients with essential hypertension. Its vasodilating and calcium antagonist effects are very slow in onset and long-lasting in all types of experimentally hypertensive models and the agent is reported to exhibit an improved side effect profile compared with other drugs of the same class. This may be explained by the slow and long-lasting inhibition of transmembrane Ca+2 uptake, which is accompanied by its very slow binding to and dissociation from the DHP receptors. A recent study in cholesterol-fed rabbits suggested that efonidipine may suppress the development of atherosclerosis without affecting the plasma lipids. Clinical trials for angina, peetoris, and for cerebrovasodilatory disorders have been reported.

Originator

Nissan Chemical (Japan)

Uses

Efonidipine Hydrochloride Monoethanolate is a potent inhibitor of the L-type calcium channel.

Brand name

Landel

Biological Activity

Selective blocker of L-type and T-type Ca 2+ channels. Displays minimal inhibition of N- and P/Q-type channels and no inhibition of R-type channels. R (-) and S (+)-enantiomers displays different channel selectivity; S (+)-Efonidipine blocks L-type and T-type channels whereas R (-)-Efonidipine displays selectivity for T-type channels. Exhibits antihypertensive activity.

InChI:InChI=1/C34H38N3O7P.C2H6O.ClH/c1-24-30(33(38)42-19-18-36(28-15-9-6-10-16-28)21-26-12-7-5-8-13-26)31(27-14-11-17-29(20-27)37(39)40)32(25(2)35-24)45(41)43-22-34(3,4)23-44-45;1-2-3;/h5-17,20,31,35H,18-19,21-23H2,1-4H3;3H,2H2,1H3;1H